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HRID 22472作成日:2026年10月26日

Dimethylformamide → (2Z)-2-(5-amino-1,2,4-thiadiazol-3-yl)-2-methoxyiminoacetyl chloride

https://huagongshe.com/reaction/22472

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物Phosphorus oxychlorideHCID 24813—
反応物2-(5-Amino-1,2,4-thiadiazol-3-yl)-2-(methoxyimino)acetic acidHCID 10130412—
溶媒1,2-DimethoxyethaneHCID 8071—
生成物(2Z)-2-(5-amino-1,2,4-thiadiazol-3-yl)-2-methoxyiminoacetyl chlorideHCID 10198354—

反応手順

In 50.0 ml of 1,2-dimethoxyethane (DME), 10.0 g of 2- (5-amino-1,2,4-thiadiazol-3-yl)-2(Z)-methoxyiminoacetic acid were stirred at -20° C., followed by the dropwise addition of a chlorinating reagent, which had been prepared beforehand by gradually adding 8.4 g of phosphorus oxychloride at 5° C. to a mixture of 20 ml of DME and 4.0 g of N,N-dimethylformamide (DMF) and then reacting them for 30 minutes. After they were reacted for 5 minutes, the reaction mixture was poured into 160 ml of ice water to precipitate crystals. The resulting crystals were collected by filtration, washed with 200 ml of ice water and then stirred for 30 minutes in 120 ml of n-hexane. After filtration, the resulting crystals were dried under reduced pressure, whereby the title compound was obtained. Yield: 8.43 g (76.6%). Purity: 97.2%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05428173
出典データセットuspto-grants-1995_06
ORD IDord-0757c3bbfa1d443bb6f3447a86ec152b
出典メモuspto-grants-1995_06